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Summary Anatomy Item Literature (10508) Expression Attributions Wiki
XB-ANAT-661

Papers associated with anatomical cluster (and tbx1)

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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;             


Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.                  


Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):                                               


The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.                                  


Timing is everything: Reiterative Wnt, BMP and RA signaling regulate developmental competence during endoderm organogenesis., Rankin SA, Rankin SA., Dev Biol. February 1, 2018; 434 (1): 121-132.          


Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M., Dev Biol. June 15, 2017; 426 (2): 301-324.                          


Genomic integration of Wnt/β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs., Stevens ML., Development. April 1, 2017; 144 (7): 1283-1295.                            


RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.      


Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty., Grieb M., PLoS One. July 16, 2015; 10 (7): e0131832.        


The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.                                            


Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.                


Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 17, 2014; 9 (1): e87294.                


Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.                  


New developments in the second heart field., Zaffran S., Differentiation. July 1, 2012; 84 (1): 17-24.


Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    


ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus., Tran HT., Dev Dyn. December 1, 2011; 240 (12): 2680-7.                


Tbx5 overexpression favors a first heart field lineage in murine embryonic stem cells and in Xenopus laevis embryos., Herrmann F., Dev Dyn. December 1, 2011; 240 (12): 2634-45.  


PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.                          


Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns., Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.              


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.                    


Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.          


The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors., Hitachi K., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.                    


The mych gene is required for neural crest survival during zebrafish development., Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.                


SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG., Development. November 1, 2007; 134 (22): 4119-30.    


Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis., Showell C., Dev Dyn. June 1, 2006; 235 (6): 1623-30.                      


Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.                        


XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.                  


The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.            


Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene., Chieffo C., Genomics. August 1, 1997; 43 (3): 267-77.

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